MX2016004742A - DERIVATIVES OF PIRIDIL KETONE, METHOD OF PREPARATION OF THE SAME, AND THE PHARMACEUTICAL APPLICATION OF THE SAME. - Google Patents
DERIVATIVES OF PIRIDIL KETONE, METHOD OF PREPARATION OF THE SAME, AND THE PHARMACEUTICAL APPLICATION OF THE SAME.Info
- Publication number
- MX2016004742A MX2016004742A MX2016004742A MX2016004742A MX2016004742A MX 2016004742 A MX2016004742 A MX 2016004742A MX 2016004742 A MX2016004742 A MX 2016004742A MX 2016004742 A MX2016004742 A MX 2016004742A MX 2016004742 A MX2016004742 A MX 2016004742A
- Authority
- MX
- Mexico
- Prior art keywords
- same
- preparation
- piridil
- ketone
- derivatives
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- -1 OF PIRIDIL KETONE Chemical class 0.000 title 1
- 150000002576 ketones Chemical class 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000002829 mitogen activated protein kinase inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/443—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La presente invención se refiere a derivados de cetona pirídicos, el método de preparación de los mismos, y la aplicación farmacéutica de los mismos. Específicamente la presente invención se refiere a derivados cetona pirídicos representados por la general (I) y las sales de los mismos, método de preparación de los mismos y usos de los mismos como inhibidores de MEK y especialmente como agentes terapéuticos para cáncer, donde las definiciones de los sustituyentes en la fórmula general (I) son las mismas como la definición en la descripción. (ver Fórmula).The present invention relates to pyridic ketone derivatives, the method of preparation thereof, and the pharmaceutical application thereof. Specifically, the present invention relates to pyridic ketone derivatives represented by general (I) and salts thereof, method of preparation thereof and uses thereof as MEK inhibitors and especially as therapeutic agents for cancer, where definitions of the substituents in the general formula (I) are the same as the definition in the description. (see Formula).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310512377 | 2013-10-25 | ||
| PCT/CN2014/085976 WO2015058589A1 (en) | 2013-10-25 | 2014-09-05 | Pyridic ketone derivatives, method of preparing same, and pharmaceutical application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2016004742A true MX2016004742A (en) | 2016-12-09 |
| MX377816B MX377816B (en) | 2025-03-11 |
Family
ID=52992223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2016004742A MX377816B (en) | 2013-10-25 | 2014-09-05 | PYRIDIL KETONE DERIVATIVES, METHOD OF PREPARING THE SAME, AND THEIR PHARMACEUTICAL APPLICATION. |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US9914703B2 (en) |
| EP (1) | EP3061747B1 (en) |
| JP (1) | JP6403172B2 (en) |
| KR (1) | KR102222569B1 (en) |
| CN (1) | CN104936945B (en) |
| AU (1) | AU2014339527B2 (en) |
| BR (1) | BR112016007396B1 (en) |
| CA (1) | CA2927635C (en) |
| ES (1) | ES2868450T3 (en) |
| MX (1) | MX377816B (en) |
| PL (1) | PL3061747T3 (en) |
| PT (1) | PT3061747T (en) |
| RU (1) | RU2667892C2 (en) |
| TW (1) | TWI662026B (en) |
| WO (1) | WO2015058589A1 (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10118911B2 (en) * | 2015-03-27 | 2018-11-06 | Jiangsu Hengrui Medicine Co., Ltd. | P-toluenesulfonate for MEK kinase inhibitor, and crystal form thereof and preparation method therefor |
| CN104892499B (en) * | 2015-06-26 | 2017-07-21 | 江西省科学院应用化学研究所 | A kind of synthetic method of 2 pyridinone derivatives |
| WO2018095403A1 (en) * | 2016-11-25 | 2018-05-31 | 江苏恒瑞医药股份有限公司 | Pyridone derivative pharmaceutical composition and preparation method thereof |
| TW201821408A (en) * | 2016-12-01 | 2018-06-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | Preparation method for pyridic ketone derivatives and intermediate thereof |
| CN108314645A (en) * | 2017-01-18 | 2018-07-24 | 上海映诺济生物科技有限公司 | One kind has compound, preparation method and the purposes of antiproliferation |
| AU2018289864B2 (en) | 2017-06-23 | 2022-03-31 | Cstone Pharmaceuticals | Coumarin-like cyclic compound as MEK inhibitor and use thereof |
| CN112912380B (en) * | 2018-12-21 | 2023-08-11 | 基石药业(苏州)有限公司 | Crystal form and amorphous form of MEK inhibitor and application thereof |
| WO2020156162A1 (en) * | 2019-01-29 | 2020-08-06 | 贝达药业股份有限公司 | Mek inhibitor and pharmaceutical use thereof |
| CN111514140B (en) * | 2019-02-01 | 2021-09-03 | 江苏恒瑞医药股份有限公司 | Application of MEK inhibitor and androgen receptor antagonist in preparation of tumor treatment drug |
| JP2022526713A (en) | 2019-03-21 | 2022-05-26 | オンクセオ | Dbait molecule in combination with a kinase inhibitor for the treatment of cancer |
| TW202114994A (en) * | 2019-07-29 | 2021-04-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | Preparation method of 1,6-dihydropyridine-3-formamide derivative |
| TW202114667A (en) * | 2019-09-11 | 2021-04-16 | 大陸商江蘇恒瑞醫藥股份有限公司 | Use of combination of mek inhibitor and cdk4/6 inhibitor in preparing medicine for treating tumor |
| KR20220098759A (en) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | A method of treating cancer that has acquired resistance to a kinase inhibitor |
| AR121078A1 (en) | 2020-01-22 | 2022-04-13 | Chugai Pharmaceutical Co Ltd | ARILAMIDE DERIVATIVES WITH ANTI-TUMOR ACTIVITY |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| CN111848613B (en) * | 2020-08-11 | 2021-09-24 | 山东大学 | A kind of diarylpyrimidine pyridone derivatives and preparation method and application thereof |
| JP7530596B2 (en) * | 2021-04-14 | 2024-08-08 | 塩野義製薬株式会社 | Triazine derivatives having an inhibitory effect on viral proliferation and pharmaceutical compositions containing the same |
| CN114605408B (en) * | 2022-03-30 | 2023-06-16 | 沈阳药科大学 | 5-hydroxy-1, 3-disubstituted phenylpyrido [2,3-d ] pyrimidine compound and preparation method and application thereof |
| TW202404581A (en) * | 2022-05-25 | 2024-02-01 | 美商醫肯納腫瘤學公司 | Mek inhibitors and uses thereof |
| WO2025073765A1 (en) | 2023-10-03 | 2025-04-10 | Institut National de la Santé et de la Recherche Médicale | Methods of prognosis and treatment of patients suffering from melanoma |
| CN120441478A (en) * | 2024-02-07 | 2025-08-08 | 成都赜灵生物医药科技有限公司 | A six-membered lactam compound and its application |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003005969A2 (en) * | 2001-07-12 | 2003-01-23 | Bristol-Myers Squibb Pharma Company | Tetrahydropurinones as corticotropin releasing factor |
| US7732616B2 (en) * | 2003-11-19 | 2010-06-08 | Array Biopharma Inc. | Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof |
| PL1761528T3 (en) | 2004-06-11 | 2008-05-30 | Japan Tobacco Inc | 5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2h-pyrido[2,3-d]pyrimidine derivatives and related compounds for the treatment of cancer |
| NZ563707A (en) * | 2005-05-18 | 2011-01-28 | Array Biopharma Inc | Heterocyclic inhibitors of MEK and methods of use thereof |
| CN101389609B (en) * | 2006-02-22 | 2012-01-11 | 霍夫曼-拉罗奇有限公司 | Hydantoin-based kinase inhibitors |
| US7612212B2 (en) * | 2006-02-22 | 2009-11-03 | Hoffmann-La Roche Inc. | Substituted hydantoins |
| CA2727252A1 (en) | 2008-07-01 | 2010-01-07 | Genentech, Inc. | Isoindolone derivatives as mek kinase inhibitors and methods of use |
| CN102134218A (en) * | 2009-06-15 | 2011-07-27 | 凯美隆(北京)药业技术有限公司 | 6-aryl amino pyridone sulfamide and 6-aryl amino pymetrozine sulfamide methyl ethyl ketone (MEK) inihibitor |
| US20120238599A1 (en) * | 2011-03-17 | 2012-09-20 | Chemizon, A Division Of Optomagic Co., Ltd. | Heterocyclic compounds as mek inhibitors |
| US20140228418A1 (en) * | 2011-05-23 | 2014-08-14 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitory compounds with mek inhibitors |
| JP6431770B2 (en) * | 2012-03-14 | 2018-11-28 | ルピン・リミテッド | Heterocyclyl compounds as MEK inhibitors |
-
2014
- 2014-09-05 CA CA2927635A patent/CA2927635C/en not_active Expired - Fee Related
- 2014-09-05 ES ES14854930T patent/ES2868450T3/en active Active
- 2014-09-05 PL PL14854930T patent/PL3061747T3/en unknown
- 2014-09-05 KR KR1020167012819A patent/KR102222569B1/en not_active Expired - Fee Related
- 2014-09-05 RU RU2016118753A patent/RU2667892C2/en active
- 2014-09-05 PT PT148549306T patent/PT3061747T/en unknown
- 2014-09-05 WO PCT/CN2014/085976 patent/WO2015058589A1/en not_active Ceased
- 2014-09-05 JP JP2016518444A patent/JP6403172B2/en not_active Expired - Fee Related
- 2014-09-05 AU AU2014339527A patent/AU2014339527B2/en not_active Ceased
- 2014-09-05 CN CN201480003661.8A patent/CN104936945B/en active Active
- 2014-09-05 BR BR112016007396-7A patent/BR112016007396B1/en not_active IP Right Cessation
- 2014-09-05 EP EP14854930.6A patent/EP3061747B1/en active Active
- 2014-09-05 MX MX2016004742A patent/MX377816B/en unknown
- 2014-09-05 US US15/030,125 patent/US9914703B2/en active Active
- 2014-09-25 TW TW103133170A patent/TWI662026B/en not_active IP Right Cessation
-
2017
- 2017-09-28 US US15/719,138 patent/US10064848B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| MX377816B (en) | 2025-03-11 |
| TW201518278A (en) | 2015-05-16 |
| CA2927635C (en) | 2021-07-20 |
| US9914703B2 (en) | 2018-03-13 |
| CN104936945A (en) | 2015-09-23 |
| RU2667892C2 (en) | 2018-09-25 |
| JP2016534027A (en) | 2016-11-04 |
| US10064848B2 (en) | 2018-09-04 |
| KR102222569B1 (en) | 2021-03-05 |
| HK1212980A1 (en) | 2016-06-24 |
| JP6403172B2 (en) | 2018-10-10 |
| EP3061747A1 (en) | 2016-08-31 |
| EP3061747B1 (en) | 2021-04-07 |
| EP3061747A4 (en) | 2017-05-10 |
| KR20160074554A (en) | 2016-06-28 |
| US20160244410A1 (en) | 2016-08-25 |
| RU2016118753A (en) | 2017-11-29 |
| ES2868450T3 (en) | 2021-10-21 |
| WO2015058589A1 (en) | 2015-04-30 |
| PL3061747T3 (en) | 2021-07-19 |
| BR112016007396B1 (en) | 2021-01-19 |
| BR112016007396A2 (en) | 2017-08-01 |
| CN104936945B (en) | 2017-11-03 |
| CA2927635A1 (en) | 2015-04-30 |
| AU2014339527B2 (en) | 2018-07-19 |
| AU2014339527A1 (en) | 2016-05-12 |
| US20180016236A1 (en) | 2018-01-18 |
| TWI662026B (en) | 2019-06-11 |
| PT3061747T (en) | 2021-05-04 |
| RU2016118753A3 (en) | 2018-05-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2016004742A (en) | DERIVATIVES OF PIRIDIL KETONE, METHOD OF PREPARATION OF THE SAME, AND THE PHARMACEUTICAL APPLICATION OF THE SAME. | |
| ECSP20033467A (en) | MACROCYCLIC COMPOUNDS TO TREAT DISEASES | |
| MX2023001876A (en) | Rapamycin derivatives. | |
| CL2018003681A1 (en) | Boronic acid derivatives and therapeutic uses thereof | |
| DOP2015000241A (en) | BIARIL-AMIDA COMPOUNDS AS CINASA INHIBITORS | |
| CR20150472A (en) | USE OF PIRAZOLOPIRIMIDINE DERIVATIVES FOR THE TREATMENT OF PI3Kd-RELATED DISORDERS | |
| CU20180152A7 (en) | PYRIMIDIN-2-ILAMINO-1H-PYRAZOLES USEFUL AS LRRK2 INHIBITORS | |
| DOP2014000204A (en) | HETEROCICLYL COMPOUNDS AS MEK INHIBITORS | |
| UY35663A (en) | DERIVATIVES OF PIPERIDINIL-INDOL AS INHIBITORS OF COMPLEMENT FACTOR B AND USES OF THE SAME | |
| MX2016014547A (en) | Compounds for treating spinal muscular atrophy. | |
| GT201400290A (en) | FUNGICIDE HETEROCICLIC CARBOXAMIDS | |
| GT201400178A (en) | OXAZOLIDIN-2-ONA COMPOUNDS AND USES OF THE SAME AS INHIBITORS OF THE PI3KS | |
| ECSP15045801A (en) | 6-(5-HYDROXY-1H-PYRAZOLE-1-IL)NICOTINAMIDE PHD INHIBITORS | |
| ECSP14013215A (en) | NEW COMPOUNDS | |
| CR20160072A (en) | COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF THE MEK | |
| UY35551A (en) | HETEROARILE DERIVATIVES AS INHIBITORS OF ALDOSTERONA SINTASA | |
| MX2016005142A (en) | DERIVATIVES OF PIRAZOLOPIRIMIDONA OR PIRROLOTRIAZONA, METHOD AND PREPARATION OF THE SAME AND PHARMACEUTICAL APPLICATIONS OF THE SAME. | |
| CO2017003955A2 (en) | 1-Alkyl-6-oxo-1,6-dihydropyridin-3-yl compounds and uses thereof | |
| CO7350640A2 (en) | Dimeric compounds | |
| MX2015009479A (en) | COMPOUNDS AND METHODS TO TREAT BACTERIAL INFECTIONS. | |
| DOP2018000062A (en) | PIRIDINONA DICABOXAMIDS FOR USE AS BROMODOMINUM INHIBITORS | |
| MX2016012784A (en) | Solid pharmaceutical compositions comprising biopterin derivatives and uses of such compositions. | |
| CO2017000011A2 (en) | Quinolizinone derivatives as pi3k inhibitors | |
| UY36228A (en) | HETEROARILO DERIVATIVES AS INHIBITORS OF ALDOSTERONE SINTASA (CYP11B2) AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| AR132461A2 (en) | Piperidinyl-indole derivatives as complement factor B inhibitors and their uses |